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Glycidyl Laurate (CAS 1984-77-6)

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Alternate Names:
Glycidyl Dodecanoate; Lauric Acid Glycidyl Ester; Dodecanoic acid
Application:
Glycidyl Laurate is one of the fatty acid esters tested for carcinogenic activity
CAS Number:
1984-77-6
Molecular Weight:
256.38
Molecular Formula:
C15H28O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Glycidyl laurate, assigned CAS number 1984-77-6, is an ester formed from the reaction of glycidol and lauric acid. This compound is particularly notable in the field of polymer chemistry and materials science due to its unique properties as an epoxide. Glycidyl laurate′s structure includes an epoxide ring, which is highly reactive and capable of undergoing ring-opening reactions. This reactivity is exploited in the synthesis of polymers and resins, where glycidyl laurate acts as a precursor or a modifier to enhance certain properties of the materials, such as flexibility, adhesion, and resistance to chemicals and heat. In research, glycidyl laurate is used to study the kinetics and mechanisms of epoxy ring-opening reactions, often catalyzed by acids, bases, or nucleophiles. These studies help in understanding how the molecular structure influences the reactivity and the final properties of the polymers. Additionally, researchers utilize glycidyl laurate to fabricate novel materials with specific functionalities by incorporating the fatty acid moiety of laurate, which can impart additional characteristics like increased hydrophobicity or specific interactions with other chemical entities. Through these applications, glycidyl laurate contributes significantly to advancements in materials that are tailored for specific industrial applications, ranging from coatings to advanced composite materials


Glycidyl Laurate (CAS 1984-77-6) References

  1. Determination of seven glycidyl esters in edible oils by gel permeation chromatography extraction and liquid chromatography coupled to mass spectrometry detection.  |  Dubois, M., et al. 2011. J Agric Food Chem. 59: 12291-301. PMID: 22017647
  2. Analytical approaches for MCPD esters and glycidyl esters in food and biological samples: a review and future perspectives.  |  Crews, C., et al. 2013. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 30: 11-45. PMID: 23020628
  3. Application of gastrointestinal modelling to the study of the digestion and transformation of dietary glycidyl esters.  |  Frank, N., et al. 2013. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 30: 69-79. PMID: 23083414
  4. Analytical method for the trace determination of esterified 3- and 2-monochloropropanediol and glycidyl fatty acid esters in various food matrices.  |  Samaras, VG., et al. 2016. J Chromatogr A. 1466: 136-47. PMID: 27623063
  5. Assessment of critical steps of a GC/MS based indirect analytical method for the determination of fatty acid esters of monochloropropanediols (MCPDEs) and of glycidol (GEs).  |  Zelinkova, Z., et al. 2017. Food Control. 77: 65-75. PMID: 28674464
  6. 1-Laurin-3-Palmitin as a Novel Matrix of Solid Lipid Particles: Higher Loading Capacity of Thymol and Better Stability of Dispersions Than Those of Glyceryl Monostearate and Glyceryl Tripalmitate.  |  Shi, H., et al. 2019. Nanomaterials (Basel). 9: PMID: 30934814
  7. Determination of 3-monochloropropanediol esters and glycidyl esters in fatty matrices by ultra-high performance liquid chromatography-tandem mass spectrometry.  |  Hidalgo-Ruiz, JL., et al. 2021. J Chromatogr A. 1639: 461940. PMID: 33548662
  8. Development of UHPLC/Q-TOF Analysis Method to Screen Glycerin for Direct Detection of Process Contaminants 3-Monochloropropane-1,2-diol Esters (3-MCPDEs) and Glycidyl Esters (GEs).  |  Girard, L., et al. 2021. Molecules. 26: PMID: 33922286
  9. Simultaneous determination of 24 congeners of 2- and 3-monochloropropanediol esters and 7 congeners of glycidyl esters using direct multi-residue analytical LC-MS/MS methods in various food matrices.  |  Lee, CC., et al. 2023. J Food Drug Anal. 31: 55-72. PMID: 37224555
  10. Preparation of 1, 3‐diacylglycerols and 1‐alkyl‐3‐acylglycerols in the presence of quaternary ammonium salt  |  Ikeda, I., Gu, X. P., Miyamoto, I., & Okahara, M. 1989. Journal of the American Oil Chemists' Society. 66(6): 822-824.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Glycidyl Laurate, 100 mg

sc-397430
100 mg
$320.00